Canonical Allele Identifier: PA2828131965
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16152
ClinVar RCV Id: RCV000017534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351109.1:p.Ile747Met
CA126227
NM_001364180.2:c.2241T>G